Variant report

Variant rs35465283
Chromosome Location chr6:140498101-140498102
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:140495600-140499200 Weak transcription NHLF lung
2 chr6:140495600-140499800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:140495800-140498200 Strong transcription K562 blood
4 chr6:140495800-140499400 Weak transcription Muscle Satellite Cultured Cells --
5 chr6:140496000-140499200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr6:140496200-140501200 Weak transcription Placenta Placenta
7 chr6:140496800-140499200 Weak transcription Osteobl bone
8 chr6:140497000-140498600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:140497000-140499000 Weak transcription NHDF-Ad bronchial
10 chr6:140497000-140500000 Weak transcription HMEC breast
11 chr6:140497000-140516400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:140497200-140499200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr6:140497200-140499200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
14 chr6:140497400-140499200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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